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Postpartum Haemorrhage in a Woman with Pre-eclampsia

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Postpartum Haemorrhage in a Woman with Pre-eclampsia

A 27-year-old woman, G2P1, at 38 weeks' gestation is admitted with a blood pressure of 158/104 mmHg on two readings four hours apart, 3+ proteinuria on dipstick, and a platelet count of 96,000/microlitre; liver enzymes are mildly raised and she has no headache or visual symptoms. Labour is induced with misoprostol and she delivers a 2.9 kg baby spontaneously 14 hours later after an uncomplicated second stage. Active management of the third stage includes 10 IU intramuscular oxytocin. Ten minutes after delivery of the placenta she has a brisk vaginal bleed; the uterus is soft and above the umbilicus, and estimated blood loss is 900 mL. Pulse 118/min, BP 138/88 mmHg, and she is pale and anxious. Intravenous access is in place and 1 L of Ringer's lactate is running. The placenta appears complete. Two units of packed red cells are crossmatched but not yet available.

1. Which uterotonic would you give next, and which one is contraindicated in this particular patient? Explain the pharmacology behind each choice.

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Working diagnosis: primary postpartum haemorrhage from uterine atony, in a woman with pre-eclampsia and thrombocytopenia.

Next drugs (in this order):

  1. Oxytocin infusion - 40 IU in 500 mL of isotonic crystalloid over 4 hours (after the initial bolus already given). It is the first-line agent and remains safe in hypertension.
  2. Misoprostol 800 micrograms sublingually (or 600 micrograms orally) - a prostaglandin E1 analogue, no hypertensive effect, but expect shivering and pyrexia.
  3. Carboprost (15-methyl PGF2 alpha) 250 micrograms intramuscularly, repeatable every 15 minutes to a maximum of 2 mg - reserve for failure of the above; it is contraindicated in asthma and can cause bronchospasm, so ask about asthma before giving it.

Contraindicated drug: methylergometrine (ergometrine).

  • Ergometrine is an ergot alkaloid that acts on alpha-adrenergic and serotonergic receptors and produces generalised vasoconstriction; in a woman with pre-eclampsia it can precipitate a hypertensive crisis, seizure, and intracranial haemorrhage.
  • It also causes nausea and vomiting, which is unhelpful in a patient who may need anaesthesia.
  • The fact that her BP has settled to 138/88 after delivery does not make ergometrine safe - pre-eclampsia remains the diagnosis, and a single bolus can still spike the pressure.

Trap to avoid: reaching for ergometrine because "it is a first-line uterotonic" - it is first-line only in normotensive women.

2. What non-drug and mechanical steps do you take now, and what is the correct dose and timing of tranexamic acid?

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Immediate non-drug actions in the first 10 minutes:

  1. Call for help - obstetrician, anaesthetist, haematologist, blood bank; designate a team leader and a scribe who records time-stamped blood loss.
  2. Bimanual uterine compression and uterine massage - the fastest mechanical measure while drugs are drawn up. Also catheterise: a full bladder prevents uterine contraction.
  3. Two large-bore (14–16 G) cannulae, warmed crystalloid, keep her warm, oxygen by mask, head-down if she becomes hypotensive. Monitor pulse, BP, urine output hourly.
  4. Inspect the genital tract and the placenta - the placenta looks complete, but check for a missing cotyledon and for vaginal/cervical lacerations; a laceration will not respond to uterotonics.
  5. Send full blood count, coagulation profile, fibrinogen, renal and liver function, and activate the massive haemorrhage protocol on standby rather than waiting for a further 500 mL loss.

Tranexamic acid:

  • 1 g intravenously over 10 minutes, started as soon as PPH is diagnosed and ideally within 3 hours of birth (WOMAN trial evidence).
  • A second 1 g dose can be given if bleeding continues after 30 minutes or restarts within 24 hours.
  • Do not delay transfer or other definitive treatment to give it; the benefit falls away after 3 hours.

Judgement point: in pre-eclampsia with a platelet count of 96,000, anticipate disseminated intravascular coagulation - the combination of hypertension, thrombocytopenia and haemorrhage is a set-up for it, so fibrinogen and platelet counts must be tracked, not just haemoglobin.

3. Given the platelet count of 96,000/microlitre, what else do you monitor, and at what point do you escalate to theatre? What operation would you expect?

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Monitoring:

  • Serial platelet counts and coagulation screen (PT, aPTT, fibrinogen) every 2–4 hours; a falling platelet count with a rising PT and low fibrinogen indicates DIC. Pre-eclampsia with thrombocytopenia below 100,000 plus major haemorrhage is high risk for it.
  • Watch for haemolysis, elevated liver enzymes and low platelets (HELLP) - check LDH, peripheral smear, and repeat liver enzymes; right upper quadrant pain would be a red flag for hepatic haematoma.
  • Hourly urine output (insert catheter), lactate, and clinical assessment of perfusion; keep the blood pressure controlled but avoid dropping it into the uteroplacental range.
  • Transfuse to targets rather than to a haemoglobin figure: platelets if <50,000 with ongoing bleeding, fresh frozen plasma and cryoprecipitate for fibrinogen <1.5–2 g/L.

Escalation to theatre - do not wait for collapse:

  • Ongoing bleeding despite oxytocin infusion, misoprostol and carboprost plus bimanual compression, or
  • Estimated loss approaching 1500 mL or ongoing loss >200 mL/hour, or
  • Signs of shock (tachycardia despite fluids, rising lactate, falling urine output), or
  • Suspected retained placenta - manual removal under anaesthesia.

Sequence in theatre: examination under anaesthesia and evacuation of retained products, then intrauterine balloon tamponade (or vacuum device), then laparotomy with B-Lynch compression suture or stepwise uterine devascularisation, and hysterectomy as the last resort. A balloon tamponade is the correct next step here, not hysterectomy - she is young, the uterus is atonic rather than ruptured, and the bleeding is not yet uncontrolled.